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Hydrochloric Acid → N-[3-Carbamoyl-4-[1-(4,5-dihydro-3H-pyrrol-2-yl)piperidin-4-yloxy]phenyl]-N-[3-[3-(ethoxycarbonylamino)(imino)methylphenyl]-2-(E)-propeny]methanesulfonamide Dihydrochloride

HRID 1796192
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HRID 1796192 반응식
[ClH:1].Cl.C([C:6]1[CH:7]=[C:8](/[CH:12]=[CH:13]/[CH2:14][N:15]([C:20]2[CH:25]=[CH:24][C:23]([O:26][CH:27]3[CH2:32][CH2:31][N:30]([C:33]4[CH2:37][CH2:36][CH2:35][N:34]=4)[CH2:29][CH2:28]3)=[C:22]([C:38](=[O:40])[NH2:39])[CH:21]=2)[S:16]([CH3:19])(=[O:18])=[O:17])[CH:9]=[CH:10][CH:11]=1)(=N)N.[C:41](=[O:55])([O:45][C:46]1[CH:51]=CC([N+]([O-])=O)=CC=1)OCC.C([N:58]([CH2:61]C)CC)C.Cl.C[N:65](C)C=O>ClCCl.O1CCOCC1.O>[ClH:1].[ClH:1].[C:38]([C:22]1[CH:21]=[C:20]([N:15]([CH2:14]/[CH:13]=[CH:12]/[C:8]2[CH:9]=[CH:10][CH:11]=[C:6]([NH:65][C:41]([O:45][CH2:46][CH3:51])=[O:55])[C:7]=2[CH:61]=[NH:58])[S:16]([CH3:19])(=[O:18])=[O:17])[CH:25]=[CH:24][C:23]=1[O:26][CH:27]1[CH2:32][CH2:31][N:30]([C:33]2[CH2:37][CH2:36][CH2:35][N:34]=2)[CH2:29][CH2:28]1)(=[O:40])[NH2:39]
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참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 8471TriethylamineHCID 586863Ethyl 4-nitrophenyl carbonateHCID 22180975N-[3-(3-amidinophenyl)-2-(E)-propenyl]-N-[3-carbamoyl-4-[1-(4,5-dihydro-3H-pyrrol-2-yl)piperidin-4-yloxy]phenyl]methanesulfonamide dihydrochloride

생성물 1

HCID 86593745
N-[3-Carbamoyl-4-[1-(4,5-dihydro-3H-pyrrol-2-yl)piperidin-4-yloxy]phenyl]-N-[3-[3-(ethoxycarbonylamino)(imino)methylphenyl]-2-(E)-propeny]methanesulfonamide Dihydrochloride
수율 84%

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매2회HCID 312751,4-Dioxane용매

실험 절차

To a solution of N-[3-(3-amidinophenyl)-2-(E)-propenyl]-N-[3-carbamoyl-4-[1-(4,5-dihydro-3H-pyrrol-2-yl)piperidin-4-yloxy]phenyl]methanesulfonamide dihydrochloride (0.23 g) obtained in example 99(b) in a mixture of dichloromethane (4.5 ml) and N,N-dimethylformamide (1.5 ml) were added successively ethyl 4-nitrophenyl carbonate (0.10 g) obtained in example 103 and triethylamine (0.16 ml) at room temperature, and the resulting mixture was stirred at room temperature overnight and then evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (50:0˜47:3). Subsequently, to a solution of the oily product obtained in ethanol (2 ml) was added a 4N solution of hydrogen chloride in dioxane (0.5 ml), and the resulting mixture was evaporated to dryness in vacuo. The amorphous solid obtained was dissolved in dichloromethane, and the resulting mixture was extracted with 1N hydrochloric acid, and the aqueous layer collected was evaporated in vacuo. The residue obtained was dissolved in water and then lyophilized to afford the title compound (0.20 g, yield: 84%) as a colorless amorphous solid.

후처리

  1. customevaporated in vacuo
  2. customThe residue obtained
  3. customwas purified by chromatography on a silica gel column
  4. customSubsequently, to a solution of the oily product obtained in ethanol (2 ml)
  5. customthe resulting mixture was evaporated to dryness in vacuo
  6. customThe amorphous solid obtained
  7. extractionthe resulting mixture was extracted with 1N hydrochloric acid
  8. customthe aqueous layer collected
  9. customwas evaporated in vacuo
  10. customThe residue obtained

출처 및 근거

ORD 기록
ord-de93b66ab61d41a6949b572767a08711
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07030138B2

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